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TRANS-4-HYDROXYMETHYL-3,5-DIPHENYL-4,5-DIHYDROISOXAZOLE
SpectraBase Compound ID 29lbK747QnT
InChI InChI=1S/C16H15NO2/c18-11-14-15(12-7-3-1-4-8-12)17-19-16(14)13-9-5-2-6-10-13/h1-10,14,16,18H,11H2/t14-,16+/m0/s1
InChIKey VILXTMZJLXFIIV-GOEBONIOSA-N
Mol Weight 253.3 g/mol
Molecular Formula C16H15NO2
Exact Mass 253.110279 g/mol
Enantiomer InChIKey VILXTMZJLXFIIV-ZBFHGGJFSA-N
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QA-47-195-4
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • TRANS-3,5-DIPHENYL-2-ISOXAZOLINE-4-METHANOL
  • [(4R,5S)-3,5-diphenyl-2-isoxazolin-4-yl]methanol
Title Journal or Book Year
Microwave Accelerated Cycloaddition Reactions of Nitrile Oxides and Allylic Alcohols Journal of the Chinese Chemical Society 2000
First Successful Metal Coordination Control in 1,3-Dipolar Cycloadditions. High-Rate Acceleration and Regio- and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols Journal of the American Chemical Society 1994

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